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carboxylic acid → acyl chloride + H3PO4 (3)
nucleophilic substitution, PCl3, heat
carboxylic acid → acyl chloride + POCl3 (3)
nucleophilic substitution, PCl5, room temp
carboxylic acid → acyl chloride + SO2 + HCl (2)
nucleophilic substitution, SOCl2
methanoic acid → CO2 + H2O (3) (K2)
oxidation, acidified K2Cr2O7, orange to green colour change
methanoic acid → CO2 + H2O (3) (K)
oxidation, acidified KMnO4, purple to colourless colour change
methanoic acid → CO2 + H2O (3) (feh)
oxidation, fehling’s solution, red ppt forms
methanoic acid → CO2 + H2O (3) (tol)
oxidation, tollens reagent, silver mirror forms
ethandoic acid → 2CO2 + 2H2O (2)
oxidation, warm acidified KMnO4
methylbenzene → benzoic acid (3)
oxidation, hot alkaline KMnO4, followed by addition of dilute HCl to acidify product